Aluminium lithium hydride → 5-methyl-3-(pyrrolidin-3-yl)-1H-indole

HRID 1526161ノート

反応式

HRID 1526161 の反応式
[H-].[Al+3].[Li+].[H-].[H-].[H-].[CH3:7][C:8]1[CH:9]=[C:10]2[C:14](=[CH:15][CH:16]=1)[NH:13][CH:12]=[C:11]2[CH:17]1[CH2:21][C:20](=O)[NH:19][C:18]1=O>C1COCC1>[CH3:7][C:8]1[CH:9]=[C:10]2[C:14](=[CH:15][CH:16]=1)[NH:13][CH:12]=[C:11]2[CH:17]1[CH2:21][CH2:20][NH:19][CH2:18]1

参加物

4

反応物 2

HCID 21226445Aluminium lithium hydrideHCID 670364713-(5-methyl-1H-indol-3-yl)pyrrolidine-2,5-dione

生成物 1

HCID 548571365-methyl-3-(pyrrolidin-3-yl)-1H-indole

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

Lithium aluminum hydride (7.9 g, 200 mmol) in dry THF (380 mL) was stirred for 20 min. at RT under nitrogen atmosphere. 3-(5-Methyl-1H-indol-3-yl) pyrrolidine-2,5-dione (9.5 g, 41 mmol) was added portionwise and the reaction mixture was heated to reflux overnight. The reaction mixture was cooled to RT, quenched with aqueous sodium sulfate, and filtered. The solid was rinsed with THF and the THF layer was dried over anhydrous sodium sulfate and evaporated under reduced pressure. The residue was purified by silica gel chromatography (25% MeOH/DCM/ammonia) to afford the title compound. Yield: 4.2 g, 49.2%.

後処理

  1. temperaturethe reaction mixture was heated
  2. temperatureto reflux overnight
  3. customquenched with aqueous sodium sulfate
  4. filtrationfiltered
  5. washThe solid was rinsed with THF
  6. dry with materialthe THF layer was dried over anhydrous sodium sulfate
  7. customevaporated under reduced pressure
  8. customThe residue was purified by silica gel chromatography (25% MeOH/DCM/ammonia)

出典と根拠

ORDレコード
ord-94cff7cb40044d7c9792b5114600280d
出典データセット
uspto-grants-2015_07
特許番号
US09085580B2

反応ノート

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